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Haematologica|September 5, 2007
Factor XI/ADAMTS13 complexes are quantitatively insignificant in human plasmaPatricia J Anderson, David Gailani, Hendrik B Feys, et al.
Biochemical and Biophysical Research Communications|December 13, 2005
Identification of amino acid residues essential for heparin binding by the A1 domain of human von Willebrand factorTatsuya Adachi, Tadashi Matsushita, Zhengyu Dong, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 27, 2007
Two Cys residues essential for von Willebrand factor multimer assembly in the GolgiAngie R Purvis, Julia Gross, Luke T Dang, et al.
International Journal of Hematology|March 29, 2008
Identification of amino acid residues responsible for von Willebrand factor binding to sulfatide by charged-to-alanine-scanning mutagenesisTakayuki Nakayama, Tadashi Matsushita, Koji Yamamoto, et al.
The Journal of Biological Chemistry|February 20, 2014
Single particle tracking of ADAMTS13 (a disintegrin and metalloprotease with thrombospondin type-1 repeats) molecules on endothelial von Willebrand factor stringsKaren De Ceunynck, Susana Rocha, Simon F De Meyer, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 10, 2008
Assembly of Weibel-Palade body-like tubules from N-terminal domains of von Willebrand factorRen-Huai Huang, Ying Wang, Robyn Roth, et al.
Thrombosis and Haemostasis|April 8, 2016
The functions of the A1A2A3 domains in von Willebrand factor include multimerin 1 bindingD'Andra N Parker, Subia Tasneem, Richard W Farndale, et al.
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